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Terminated Phase 1Phase 2 Interventional Accepts healthy volunteers Results available

Safety and Immunogenicity of a Single Dose of the Recombinant Live-Attenuated Respiratory Syncytial Virus (RSV) Vaccines RSV ΔNS2/Δ1313/I1314L, RSV 6120/ΔNS2/1030s, RSV 276 or Placebo, Delivered as Nose Drops to RSV-Seronegative Children 6 to 24 Months of Age

ClinicalTrials.gov ID: NCT03916185

Public ClinicalTrials.gov record NCT03916185. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 6, 2026, 4:26 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized Phase I/II Study of the Safety and Immunogenicity of a Single Dose of the Recombinant Live-Attenuated Respiratory Syncytial Virus (RSV) Vaccines RSV ΔNS2/Δ1313/I1314L, RSV 6120/ΔNS2/1030s, RSV 276 or Placebo, Delivered as Nose Drops to RSV-Seronegative Children 6 to 24 Months of Age

Study identification

NCT ID
NCT03916185
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Enrollment
67 participants

Conditions and interventions

Interventions

  • Placebo Biological
  • RSV 276 Vaccine Biological
  • RSV 6120/ΔNS2/1030s Vaccine Biological
  • RSV ΔNS2/Δ1313/I1314L Vaccine Biological

Biological

Eligibility (public fields only)

Age range
6 Months to 25 Months
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 19, 2019
Primary completion
Jan 21, 2024
Completion
Apr 24, 2024
Last update posted
Feb 20, 2025

2019 – 2024

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
David Geffen School of Medicine at UCLA NICHD CRS Los Angeles California 90095-1752
University of California, UC San Diego CRS- Mother-Child-Adolescent HIV Program San Diego California 92103
Univ. of Colorado Denver NICHD CRS Aurora Colorado 80045
Emory University School of Medicine NICHD CRS Atlanta Georgia 30322
Rush Univ. Cook County Hosp. Chicago NICHD CRS Chicago Illinois 60612
Lurie Children's Hospital of Chicago (LCH) CRS Chicago Illinois 60614-3393
University of Maryland School of Medicine Center for Vaccine Development CRS Baltimore Maryland 21201
The Children's Mercy Hospital CRS Kansas City Missouri 64108-4619
Center for Vaccine Development CRS St Louis Missouri 63104
SUNY Stony Brook NICHD CRS Stony Brook New York 11794
Jacobi Med. Ctr. Bronx NICHD CRS The Bronx New York 10461
Duke Vaccine and Trials Unit CRS Durham North Carolina 27703
Gamble Center for Clinical Studies CRS Cincinnati Ohio 45229
Baylor College of Medicine/ Texas Children's Hospital NICHD CRS Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03916185, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 20, 2025 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03916185 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →